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QC Analyst, Microbiology

Employer
Proclinical Staffing
Location
Feasterville, Pennsylvania, US
Salary
Competitive
Closing date
May 16, 2024
View more categoriesView less categories
Sector
Consultancy/Private Sector
Field
Conservation science
Discipline
Biology
Salary Type
Salary
Employment Type
Full time

QC Analyst, Microbiology - Contract - Philadelphia, PA

Proclinical is seeking a dedicated and detail-oriented QC Analyst, Microbiology. This is a contract position located in Philadelphia, PA.

Primary Responsibilities:

The successful candidate will support quality control testing operations, focusing on in-process and final drug product microbial testing. This role requires a commitment to a weekend 2nd shift to support manufacturing weekend activities.

Skills & Requirements:
  • Bachelor's degree in a relevant discipline (biological sciences or equivalent).
  • Experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus.
  • Ability to interface with multi-disciplined teams.
  • Detail-oriented with strong technical skills.
  • Ability to manage multiple priorities involving aggressive timelines.
  • High level of ownership and accountability.
  • Ability to recognize time sensitivity.
  • Ability to wear appropriate clean room attire and all Personal Protective Equipment (PPE).
  • Ability to meet physical demands such as standing/walking for most of the day, climbing ladders or steps, and lifting/carrying objects weighing 45 pounds.
  • Comfortable working in both an office and a manufacturing lab setting, with potential exposure to various chemical/biochemical exposures, noise, equipment hazards, and strong odors.

The QC Analyst will:
  • Perform daily cGMP quality control laboratory microbiological testing activities.
  • Conduct environmental monitoring of the cleanroom areas as scheduled.
  • Analyze data and report results of microbiology assays to support product lot release.
  • Ensure all activities comply with cGMP.
  • Conduct thorough cGMP investigations for out-of-specification test results.
  • Perform Environmental monitoring Data trending.
  • Support technical problem solving.
  • Support product stability programs including execution of stability testing, stability data analysis, and final reporting of stability data.
  • Maintain a high level of efficiency, producing high quality and accurate results.


If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at (+1) 267-428-7770 or m.raletz@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

INDSCIC

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